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Life-long epigenetic programming of cortical architecture by maternal 'Western' diet during pregnancy.
Cinquina, Valentina; Calvigioni, Daniela; Farlik, Matthias; Halbritter, Florian; Fife-Gernedl, Victoria; Shirran, Sally L; Fuszard, Matthew A; Botting, Catherine H; Poullet, Patrick; Piscitelli, Fabiana; Máté, Zoltán; Szabó, Gábor; Yanagawa, Yuchio; Kasper, Siegfried; Di Marzo, Vincenzo; Mackie, Ken; McBain, Chris J; Bock, Christoph; Keimpema, Erik; Harkany, Tibor.
Afiliação
  • Cinquina V; Department of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
  • Calvigioni D; Department of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
  • Farlik M; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
  • Halbritter F; Department of Dermatology, Medical University of Vienna, Vienna, Austria.
  • Fife-Gernedl V; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
  • Shirran SL; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
  • Fuszard MA; School of Chemistry, University of St. Andrews, St. Andrews, United Kingdom.
  • Botting CH; School of Chemistry, University of St. Andrews, St. Andrews, United Kingdom.
  • Poullet P; Faculty of Medicine, Martin-Luther University, Halle-Wittenberg, Halle, Germany.
  • Piscitelli F; School of Chemistry, University of St. Andrews, St. Andrews, United Kingdom.
  • Máté Z; Institut Curie & INSERM U900, Paris, France.
  • Szabó G; Endocannabinoid Research Group, Institute of Biomolecular Chemistry (ICB), National Research Council (CNR), Pozzuoli, Italy.
  • Yanagawa Y; Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
  • Kasper S; Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
  • Di Marzo V; Department of Genetic and Behavioral Neuroscience, Gunma University School of Medicine, Maebashi, Japan.
  • Mackie K; Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
  • McBain CJ; Endocannabinoid Research Group, Institute of Biomolecular Chemistry (ICB), National Research Council (CNR), Pozzuoli, Italy.
  • Bock C; Canada Excellence Research Chair, Institut Universitaire de Cardiologie et de Pneumologie de Québec and Institut sur la Nutrition et les Aliments Fonctionnels, Université Laval, Québec, QC, Canada.
  • Keimpema E; Department of Psychological & Brain Sciences, Indiana University, Bloomington, Indiana, USA.
  • Harkany T; Program in Developmental Neuroscience, Eunice Kennedy-Shriver National Institute of Child Health and Human Development, NIH, Bethesda, USA.
Mol Psychiatry ; 25(1): 22-36, 2020 01.
Article em En | MEDLINE | ID: mdl-31735910
ABSTRACT
The evolution of human diets led to preferences toward polyunsaturated fatty acid (PUFA) content with 'Western' diets enriched in ω-6 PUFAs. Mounting evidence points to ω-6 PUFA excess limiting metabolic and cognitive processes that define longevity in humans. When chosen during pregnancy, ω-6 PUFA-enriched 'Western' diets can reprogram maternal bodily metabolism with maternal nutrient supply precipitating the body-wide imprinting of molecular and cellular adaptations at the level of long-range intercellular signaling networks in the unborn fetus. Even though unfavorable neurological outcomes are amongst the most common complications of intrauterine ω-6 PUFA excess, cellular underpinnings of life-long modifications to brain architecture remain unknown. Here, we show that nutritional ω-6 PUFA-derived endocannabinoids desensitize CB1 cannabinoid receptors, thus inducing epigenetic repression of transcriptional regulatory networks controlling neuronal differentiation. We found that cortical neurons lose their positional identity and axonal selectivity when mouse fetuses are exposed to excess ω-6 PUFAs in utero. Conversion of ω-6 PUFAs into endocannabinoids disrupted the temporal precision of signaling at neuronal CB1 cannabinoid receptors, chiefly deregulating Stat3-dependent transcriptional cascades otherwise required to execute neuronal differentiation programs. Global proteomics identified the immunoglobulin family of cell adhesion molecules (IgCAMs) as direct substrates, with DNA methylation and chromatin accessibility profiling uncovering epigenetic reprogramming at >1400 sites in neurons after prolonged cannabinoid exposure. We found anxiety and depression-like behavioral traits to manifest in adult offspring, which is consistent with genetic models of reduced IgCAM expression, to suggest causality for cortical wiring defects. Overall, our data uncover a regulatory mechanism whose disruption by maternal food choices could limit an offspring's brain function for life.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Epigênese Genética / Dieta Ocidental Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Epigênese Genética / Dieta Ocidental Idioma: En Ano de publicação: 2020 Tipo de documento: Article